ClinVar Miner

List of variants in gene PCARE reported as benign by EGL Genetic Diagnostics, Eurofins Clinical Diagnostics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_001029883.3(PCARE):c.1844T>A (p.Val615Asp) rs140776870
NM_001029883.3(PCARE):c.184C>G (p.Pro62Ala) rs76346220
NM_001029883.3(PCARE):c.1882G>A (p.Ala628Thr) rs571059484
NM_001029883.3(PCARE):c.2063G>A (p.Cys688Tyr) rs149601594
NM_001029883.3(PCARE):c.2112T>C (p.Asn704=) rs10200693
NM_001029883.3(PCARE):c.2374C>G (p.Leu792Val) rs17744093
NM_001029883.3(PCARE):c.2499G>A (p.Pro833=) rs34253433
NM_001029883.3(PCARE):c.2875G>A (p.Ala959Thr) rs192350796
NM_001029883.3(PCARE):c.2889C>T (p.Ser963=) rs144569618
NM_001029883.3(PCARE):c.3058_3059delinsAG (p.Gln1020Arg) rs796065322
NM_001029883.3(PCARE):c.3264_3266del (p.Pro1089del) rs138020654
NM_001029883.3(PCARE):c.3291G>A (p.Gln1097=) rs183536545
NM_001029883.3(PCARE):c.3668+14T>C rs72861052
NM_001029883.3(PCARE):c.3669-2AGC[4]
NM_001029883.3(PCARE):c.3739G>A (p.Gly1247Ser) rs187333111
NM_001029883.3(PCARE):c.3789G>A (p.Leu1263=) rs199689791

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